K241635
- 510(k) number
- K241635
- Device name
- da Vinci E-200 Electrosurgical Generator
- Applicant
- Intuitive Surgical CA · US
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2024-08-05
- Date received
- 2024-06-06
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.0 MB · U.S. public domain
Also available from FDA: K241635.pdf
Official FDA record: K241635
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.